Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1296277.RACeP66dfC3O56hFtnMDwB6Zalk8OB18Cl87FAsJ5SMwg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1296277.RACeP66dfC3O56hFtnMDwB6Zalk8OB18Cl87FAsJ5SMwg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1296277.RACeP66dfC3O56hFtnMDwB6Zalk8OB18Cl87FAsJ5SMwg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1296277.RACeP66dfC3O56hFtnMDwB6Zalk8OB18Cl87FAsJ5SMwg130_provenance.
- NP1296277.RACeP66dfC3O56hFtnMDwB6Zalk8OB18Cl87FAsJ5SMwg130_assertion description "[The lack of any strong association between C4 variants and RA overall makes it unlikely that the association between RA and genes within the MHS represents a direct effect of variants within the C4A or C4B loci themselves.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1296277.RACeP66dfC3O56hFtnMDwB6Zalk8OB18Cl87FAsJ5SMwg130_provenance.
- NP1296277.RACeP66dfC3O56hFtnMDwB6Zalk8OB18Cl87FAsJ5SMwg130_assertion evidence source_evidence_literature NP1296277.RACeP66dfC3O56hFtnMDwB6Zalk8OB18Cl87FAsJ5SMwg130_provenance.
- NP1296277.RACeP66dfC3O56hFtnMDwB6Zalk8OB18Cl87FAsJ5SMwg130_assertion SIO_000772 2711369 NP1296277.RACeP66dfC3O56hFtnMDwB6Zalk8OB18Cl87FAsJ5SMwg130_provenance.
- NP1296277.RACeP66dfC3O56hFtnMDwB6Zalk8OB18Cl87FAsJ5SMwg130_assertion wasDerivedFrom befree-2016 NP1296277.RACeP66dfC3O56hFtnMDwB6Zalk8OB18Cl87FAsJ5SMwg130_provenance.
- NP1296277.RACeP66dfC3O56hFtnMDwB6Zalk8OB18Cl87FAsJ5SMwg130_assertion wasGeneratedBy ECO_0000203 NP1296277.RACeP66dfC3O56hFtnMDwB6Zalk8OB18Cl87FAsJ5SMwg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1296277.RACeP66dfC3O56hFtnMDwB6Zalk8OB18Cl87FAsJ5SMwg130_provenance.